Band Position‐Independent Piezo‐Electrocatalysis for Ultrahigh CO2 Conversion
Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo‐electrocatalysis, i.e., screening charge effect and energy band theory, general...
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Published in | Advanced materials (Weinheim) Vol. 35; no. 21; pp. e2300027 - n/a |
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Main Authors | , , , , , , , , , , , |
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Abstract | Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo‐electrocatalysis, i.e., screening charge effect and energy band theory, generally coexist in the most piezoelectrics, making the essential mechanism remain controversial. Here, for the first time, the two mechanisms in piezo‐electrocatalytic CO2 reduction reaction (PECRR) is distinguished through a narrow‐bandgap piezo‐electrocatalyst strategy using MoS2 nanoflakes as demo. With conduction band of −0.12 eV, the MoS2 nanoflakes are unsatisfied for CO2‐to‐CO redox potential of −0.53 eV, yet they achieve an ultrahigh CO yield of ≈543.1 µmol g−1 h−1 in PECRR. Potential band position shifts under vibration are still unsatisfied with CO2‐to‐CO potential verified by theoretical investigation and piezo‐photocatalytic experiment, further indicating that the mechanism of piezo‐electrocatalysis is independent of band position. Besides, MoS2 nanoflakes exhibit unexpected intense “breathing” effect under vibration and enable the naked‐eye‐visible inhalation of CO2 gas, independently achieving the complete carbon cycle chain from CO2 capture to conversion. The CO2 inhalation and conversion processes in PECRR are revealed by a self‐designed in situ reaction cell. This work brings new insights into the essential mechanism and surface reaction evolution of piezo‐electrocatalysis.
Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities, drawing great interest but also suffering from the controversial mechanisms. A narrow‐bandgap piezo‐electrocatalyst strategy is proposed by choosing CO2 reduction as a probe reaction to distinguish the two potential mechanisms, i.e., screening charge effect and energy band theory, and reveal that piezo‐electrocatalysis is independent of band positions. |
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AbstractList | Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo‐electrocatalysis, i.e., screening charge effect and energy band theory, generally coexist in the most piezoelectrics, making the essential mechanism remain controversial. Here, for the first time, the two mechanisms in piezo‐electrocatalytic CO2 reduction reaction (PECRR) is distinguished through a narrow‐bandgap piezo‐electrocatalyst strategy using MoS2 nanoflakes as demo. With conduction band of −0.12 eV, the MoS2 nanoflakes are unsatisfied for CO2‐to‐CO redox potential of −0.53 eV, yet they achieve an ultrahigh CO yield of ≈543.1 µmol g−1 h−1 in PECRR. Potential band position shifts under vibration are still unsatisfied with CO2‐to‐CO potential verified by theoretical investigation and piezo‐photocatalytic experiment, further indicating that the mechanism of piezo‐electrocatalysis is independent of band position. Besides, MoS2 nanoflakes exhibit unexpected intense “breathing” effect under vibration and enable the naked‐eye‐visible inhalation of CO2 gas, independently achieving the complete carbon cycle chain from CO2 capture to conversion. The CO2 inhalation and conversion processes in PECRR are revealed by a self‐designed in situ reaction cell. This work brings new insights into the essential mechanism and surface reaction evolution of piezo‐electrocatalysis.
Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities, drawing great interest but also suffering from the controversial mechanisms. A narrow‐bandgap piezo‐electrocatalyst strategy is proposed by choosing CO2 reduction as a probe reaction to distinguish the two potential mechanisms, i.e., screening charge effect and energy band theory, and reveal that piezo‐electrocatalysis is independent of band positions. Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo‐electrocatalysis, i.e., screening charge effect and energy band theory, generally coexist in the most piezoelectrics, making the essential mechanism remain controversial. Here, for the first time, the two mechanisms in piezo‐electrocatalytic CO2 reduction reaction (PECRR) is distinguished through a narrow‐bandgap piezo‐electrocatalyst strategy using MoS2 nanoflakes as demo. With conduction band of −0.12 eV, the MoS2 nanoflakes are unsatisfied for CO2‐to‐CO redox potential of −0.53 eV, yet they achieve an ultrahigh CO yield of ≈543.1 µmol g−1 h−1 in PECRR. Potential band position shifts under vibration are still unsatisfied with CO2‐to‐CO potential verified by theoretical investigation and piezo‐photocatalytic experiment, further indicating that the mechanism of piezo‐electrocatalysis is independent of band position. Besides, MoS2 nanoflakes exhibit unexpected intense “breathing” effect under vibration and enable the naked‐eye‐visible inhalation of CO2 gas, independently achieving the complete carbon cycle chain from CO2 capture to conversion. The CO2 inhalation and conversion processes in PECRR are revealed by a self‐designed in situ reaction cell. This work brings new insights into the essential mechanism and surface reaction evolution of piezo‐electrocatalysis. Piezo-electrocatalysis as an emerging mechano-to-chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo-electrocatalysis, i.e., screening charge effect and energy band theory, generally coexist in the most piezoelectrics, making the essential mechanism remain controversial. Here, for the first time, the two mechanisms in piezo-electrocatalytic CO2 reduction reaction (PECRR) is distinguished through a narrow-bandgap piezo-electrocatalyst strategy using MoS2 nanoflakes as demo. With conduction band of -0.12 eV, the MoS2 nanoflakes are unsatisfied for CO2 -to-CO redox potential of -0.53 eV, yet they achieve an ultrahigh CO yield of ≈543.1 µmol g-1 h-1 in PECRR. Potential band position shifts under vibration are still unsatisfied with CO2 -to-CO potential verified by theoretical investigation and piezo-photocatalytic experiment, further indicating that the mechanism of piezo-electrocatalysis is independent of band position. Besides, MoS2 nanoflakes exhibit unexpected intense "breathing" effect under vibration and enable the naked-eye-visible inhalation of CO2 gas, independently achieving the complete carbon cycle chain from CO2 capture to conversion. The CO2 inhalation and conversion processes in PECRR are revealed by a self-designed in situ reaction cell. This work brings new insights into the essential mechanism and surface reaction evolution of piezo-electrocatalysis.Piezo-electrocatalysis as an emerging mechano-to-chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over the past decade. However, the two potential mechanisms in piezo-electrocatalysis, i.e., screening charge effect and energy band theory, generally coexist in the most piezoelectrics, making the essential mechanism remain controversial. Here, for the first time, the two mechanisms in piezo-electrocatalytic CO2 reduction reaction (PECRR) is distinguished through a narrow-bandgap piezo-electrocatalyst strategy using MoS2 nanoflakes as demo. With conduction band of -0.12 eV, the MoS2 nanoflakes are unsatisfied for CO2 -to-CO redox potential of -0.53 eV, yet they achieve an ultrahigh CO yield of ≈543.1 µmol g-1 h-1 in PECRR. Potential band position shifts under vibration are still unsatisfied with CO2 -to-CO potential verified by theoretical investigation and piezo-photocatalytic experiment, further indicating that the mechanism of piezo-electrocatalysis is independent of band position. Besides, MoS2 nanoflakes exhibit unexpected intense "breathing" effect under vibration and enable the naked-eye-visible inhalation of CO2 gas, independently achieving the complete carbon cycle chain from CO2 capture to conversion. The CO2 inhalation and conversion processes in PECRR are revealed by a self-designed in situ reaction cell. This work brings new insights into the essential mechanism and surface reaction evolution of piezo-electrocatalysis. |
Author | Wang, Yang Han, Guang Gao, Xingsen Feng, Yajie Dai, Ji‐Yan Meng, Jiazhi Ban, Chaogang Gan, Li‐Yong Xiong, Xin Wu, Di Zhou, Xiaoyuan Ma, Jiangping |
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References_xml | – volume: 117 year: 2013 publication-title: J. Phys. Chem. C – volume: 6 start-page: 15 year: 1996 publication-title: Comp. Mater. Sci. – volume: 11 start-page: 7690 year: 2019 publication-title: Nanoscale – volume: 60 year: 2021 publication-title: Angew. Chem., Int. Ed. – volume: 56 52 262 start-page: 351 year: 2017 2018 2020 publication-title: Angew. Chem., Int. Ed. Nano Energy Appl Catal B – volume: 134 year: 2022 publication-title: Angew. Chem., Int. Ed. – volume: 4 start-page: 690 year: 2019 publication-title: Nat. Energy – volume: 13 33 11 start-page: 2425 1328 year: 2022 2021 2020 publication-title: Nat. Commun. Adv. Mater. Nat. Commun. – volume: 45 start-page: 44 year: 2018 publication-title: Nano Energy – volume: 3 start-page: 1063 year: 2020 publication-title: Nano Mater – volume: 586 start-page: 758 year: 2021 publication-title: J. Colloid Interf. Sci. – volume: 28 start-page: 3718 year: 2016 publication-title: Adv. Mater. – volume: 553 year: 2021 publication-title: Appl. Surf. Sci. – volume: 77 start-page: 3865 year: 1996 publication-title: Phys. Rev. Lett. – volume: 8 start-page: 76 year: 2009 publication-title: Nat. Mater. – volume: 4 start-page: 719 year: 2021 publication-title: Nat. Catal. – volume: 66 year: 2019 publication-title: Nano Energy – volume: 50 year: 1994 publication-title: Phys. Rev. B – volume: 608 51 start-page: 69 6560 year: 2022 2017 publication-title: Nature Environ. Sci. Technol. – volume: 2 start-page: 0105 year: 2018 publication-title: Nat. Rev. Chem. – volume: 6 4 start-page: 46 952 year: 2021 2021 publication-title: Nat. Energy Nat. Catal. – volume: 366 7 start-page: 1500 year: 2019 2019 publication-title: Science J. Mater. Chem. A – volume: 22 start-page: 1385 year: 2012 publication-title: Adv. Funct. Mater. – volume: 31 year: 2019 publication-title: Adv. Mater. – volume: 3 start-page: 478 year: 2020 publication-title: Nat. Catal. – volume: 3 year: 2017 – volume: 12 start-page: 3508 year: 2021 publication-title: Nat. Commun. – volume: 616 year: 2023 publication-title: Appl. Surf. Sci. – volume: 514 start-page: 470 year: 2014 publication-title: Nature – volume: 116 year: 2016 publication-title: Chem. Rev. – volume: 54 year: 1996 publication-title: Phys. Rev. B – volume: 92 year: 2022 publication-title: Nano Energy – volume: 10 33 1 year: 2020 2021 2016 publication-title: Adv. Energy Mater. Adv. Mater. Nat. Rev. Mater. – volume: 32 year: 2020 publication-title: Adv. Mater. – volume: 5 start-page: 73 year: 1998 publication-title: Ultrason. Sonochem. – volume: 131 year: 2019 publication-title: Angew. Chem., Int. Ed. – volume: 121 year: 2022 publication-title: Appl. Phys. Lett. – volume: 12 year: 2022 publication-title: Adv. Energy Mater. – volume: 140 47 year: 2018 2018 publication-title: J. Am. Chem. Soc. John Dalton Prog. Sci., Pap. Conf. Hist. Sci. – volume: 45 start-page: 90 year: 2019 publication-title: Ceram. Int. – volume: 5 year: 2019 publication-title: Sci Adv |
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Snippet | Piezo‐electrocatalysis as an emerging mechano‐to‐chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over... Piezo-electrocatalysis as an emerging mechano-to-chemistry energy conversion technique opens multiple innovative opportunities and draws great interest over... |
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SubjectTerms | Band theory Carbon cycle Carbon dioxide Carbon sequestration Chemical reduction CO 2 reduction Conduction bands Electrocatalysis Electrocatalysts energy band theory Energy bands Energy conversion Materials science Molybdenum disulfide piezo‐electrocatalysis Respiration screening charge effect Surface reactions Vibration |
Title | Band Position‐Independent Piezo‐Electrocatalysis for Ultrahigh CO2 Conversion |
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